ORTHOPEDIC PLATE SYSTEM

Description

FIELD

[0001] The present system relates to bone fixation devices. More particularly, the present system provides for an orthopedic system including a plate, and a screw system.

BACKGROUND

[0002] In the treatment of various spinal conditions, including the treatment of fractures, tumors and degenerative conditions, it is necessary to secure and stabilize the anterior column of the spine following removal of a vertebral body or part. Various devices for internal fixation of bone segments in the human or animal body are known in the art.

[0003] Following such removal made using a thoracotomy, thoracoabdominal or retroperitoneal approach, the normal anatomy is reconstructed using tricortical iliac crest or fibular strut grafts. Not only are removals performed on the thoracic spine, as is the case for the above procedures, but also the cervical spine. Once bone matter is removed, it is then necessary to secure and stabilize the graft, desirably in such a manner as to permit rapid mobilization of the patient. Such objectives can be accomplished by a bone plate. However, to accomplish this service in the optimum manner, it is necessary that the plate be reasonably congruent with the bone to which it is applied, that it have as low a profile as possible, that it be firmly secured to the spinal column so that it is not torn out when the patient places weight and stress upon it and that it be capable of placement and fixation in a manner that is convenient for the surgeon.

[0004] In this context it is necessary to secure the plate to the spinal body and also, in some cases, to the graft. Conventionally, such attachment would be by the use of screws driven through screw holes in the plate into the bone. However, when stabilizing the position of cervical vertebrae, the plate is designed to lie near and posterior to the esophagus of the patient. Due to its relative location to the esophagus and other connective tissue, if the screw securing the plate to the cervical spine backs out, the screw could irritate or even pierce the esophagus, resulting in pain, infection, and/or possible death of the patient. Consequently, anti-back out mechanisms are desired in the orthopedic plate industry.

[0005] US 6,030,389 describes a bone fixation system comprising a bone plate and a bone screw assembly. The bone plate includes a thru-bore which has an entry diameter, an intermediate diameter and an exit diameter. The intermediate diameter is larger than the entry diameter and the exit diameter. The bone screw assembly can be coupled to the thru-bore and comprises a bone screw with a head section, a thread section and a central bore. It further comprises an expandable ring coupled to the head section and a pin arranged to be at least partially disposed in the central bore. The pin includes a varying outer profile that engages the expandable ring to vary an outer diameter of the expandable ring to couple the screw assembly in the thru-bore.

[0006] US 6,039,740, US 2004/260306, US 6,575,075 and US 6,602,255 also describe boneplates and fasteners extending through passageways in the plate. The fasteners have shafts for engaging bone and heads generally adapted for locking to the plate.

SUMMARY OF INVENTION

[0007] According to the present invention, there is provided a bone fixation system comprising: a bone plate including a thru-bore having an entry diameter, an intermediate diameter, and an exit diameter, wherein said intermediate diameter is larger than said entry diameter and said exit diameter; and a bone screw assembly configured to be coupled to said thru-bore; wherein said screw assembly comprises: a bone screw having a head section, a thread section, and a central bore; an expandable ring coupled to said head section; and a pin arranged to be at least partially disposed in said central bore; wherein said pin includes a varying outer profile that engages said expandable ring to vary an outer diameter of said expandable ring to couple said screw assembly in said thru-bore; and the head section further comprising a ring channel configured to retain said expandable ring in both a relaxed position and an expanded position and wherein said pin comprises: a generally cylindrical body having a proximal end and a distal end; a graduated entry taper formed on said distal end; a first engagement diameter disposed along said body, wherein said first engagement diameter corresponds to a relaxed diameter of said expandable ring and a second engagement diameter disposed along said body between said first engagement diameter and said proximal end of said pin, wherein said second engagement diameter corresponds to an expanded diameter of said expandable ring.

[0008] Preferred embodiments of the invention are set forth in the dependent claims and are set forth in the dependent claims.

BRIEF DESCRIPTION OF THE DRAWINGS

[0009] The accompanying drawings illustrate various exemplary embodiments of the present system and are a part of the specification. Together with the following description, the drawings demonstrate and explain the principles of the present system. The illustrated embodiments are examples of the present system and do not limit the scope thereof.

FIG. 1 is a side view of an assembled cervical plate system, according to one exemplary embodiment.

FIG. 2 is an exploded view illustrating the components of the screw assembly and bone plate of the exemplary embodiment illustrated in FIG. 1.

FIGS. 3A-3C are respectively top, side, and cross-sectional views of a bone plate, according to various exemplary embodiments.

FIGS. 4A-4D are respectively a side, a bottom, a top, and a cross-sectional view of a bone screw, according to one exemplary embodiment.

FIGS. 5A and 5B are respectively a top an a side view of an expandable ring configured to be mated with a bone screw, according to one exemplary embodiment.

FIGS. 6A and 6B are a side view and a top view of a lock pin, according to one exemplary embodiment.

FIG. 7 is a flow chart illustrating a method of securing an orthopedic plate, according to one exemplary embodiment.

FIG. 8 is an enlarged cross-sectional view of a thru-bore of an orthopedic plate during installation, according to one exemplary embodiment.

FIG. 9 is an enlarged cross-sectional view of a screw system being inserted into a thru-bore of an orthopedic plate, according to one exemplary embodiment.

FIG. 10 is an enlarged cross-sectional view of a properly positioned screw system in a thru-bore of an orthopedic plate, in accordance with one exemplary embodiment.

FIG. 11 is an enlarged cross-sectional view of a screw system securely coupled to a thru-bore of an orthopedic plate, according to one exemplary embodiment.

[0010] In the drawings, identical reference numbers identify similar elements or acts. The sizes and relative positions of elements in the drawings are not necessarily drawn to scale. For example, the shapes of various elements and angles are not drawn to scale, and some of these elements are arbitrarily enlarged and positioned to improve drawing legibility. Further, the particular shapes of the elements as drawn, are not intended to convey any information regarding the actual shape of the particular elements, and have been solely selected for ease of recognition in the drawings. Throughout the drawings, identical reference numbers designate similar but not necessarily identical elements.

DETAILED DESCRIPTION

[0011] The present specification describes a system and a method for coupling an orthopedic plate to one or more bones while preventing back-out of the fastener. Further, according to one exemplary embodiment, the present specification describes the structure of an orthopedic plate system that prevents back-out of a screw while positionally fixing bone segments. Further details of the present exemplary system and method will be provided below.

[0012] By way of example, orthopedic plate systems may be used in the treatment of various spinal conditions. As mentioned, when applied to stabilize the position of cervical vertebrae, the plate portion of the orthopedic plate system is designed to lie near and posterior to the esophagus of the patient. Due to its relative location to the esophagus and other connective tissue, the top surface of the plate portion may be smooth and free of sharp corners to prevent irritation or piercing of the esophagus and surrounding tissue. Further, in order to prevent irritation and/or piercing, any connection hardware that is used to couple the plate portion to the cervical vertebrae should remain below or even with the top surface of the plate portion.

[0013] If the screw or other fastener securing the plate portion to the cervical spine backs out or otherwise protrudes above the top surface of the plate portion, the screw could irritate or even pierce the esophagus, resulting in pain, infection, and/or possible death of the patient. Consequently, the present exemplary system and method provide an orthopedic plate system including a bone plate with thru-bores having varying diameters, with the larger diameter being constrained on the top and the bottom by smaller bore diameters. Further, a screw system is described below that, when assembled, is configured to leverage the varying bore diameter of the thru-bores formed in the bone plate to prevent the screw system from backing out.

[0014] Moreover, the present exemplary system and method provides anti-back out protection with a minimal engagement surface on the bone plate. Consequently, the profile size of the bone plate, when compared to traditional orthopedic plate systems, is reduced. This reduction in profile size adds comfort to the patient by reducing the likelihood that difficulty in swallowing will develop due to the presence of the orthopedic plate system.

[0015] In the following description, certain specific details are set forth in order to provide a thorough understanding of various embodiments of the present orthopedic plate system and method.

[0016] As used in the present specification, and in the appended claims, the term "ring" or "expansion ring" shall not be interpreted as necessitating a circular cross section. Rather, as used herein and in the appended claims, the term "ring" or "expansion ring" may include any object having a substantially closed periphery regardless of the cross-sectional profile. The term "ring" shall include objects having flat sided profiles, curvilinear profiles, and/or profiles defined by a varying radius.

[0017] Additionally the term "pin" shall be interpreted broadly to include any elongate member, and is not limited to cylindrical elongate members. Rather, as used herein and in the appended claims, the term "pin" shall apply to elongate members having a circular, a quadratic, and/or non-symmetric cross-sectional profile.

[0018] Unless the context requires otherwise, throughout the specification and claims which follow, the word "comprise" and variations thereof, such as, "comprises" and "comprising" are to be construed in an open, inclusive sense, that is as "including, but not limited to."

[0019] Reference in the specification to "one embodiment" or "an embodiment" means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment. The appearance of the phrase "in one embodiment" in various places in the specification are not necessarily all referring to the same embodiment. Furthermore, the particular features, structures, or characteristics may be combined in any suitable manner in one or more embodiments.

Exemplary Structure

[0020] FIG. 1 illustrates an assembled cervical plate system (100), according to one exemplary embodiment. As illustrated, the exemplary cervical plate system (100) includes a number of components including, but in no way limited to, a bone plate (110) and at least one screw assembly (120) coupled to the bone plate (110). According to the exemplary embodiment illustrated in FIG. 1, the screw assemblies (120) are configured to be securely coupled to a patient's bone(s) while securely coupling to the bone plate (110) to provide structural and positional stability while preventing issues with the screw assembly backing out. Further, as illustrated in FIG. 1, the exemplary cervical plate system (100), when assembled, maintains the highest point of the screw assembly (120) below the highest surface of the bone plate (110).

[0021] FIG. 2 is an exploded view of the exemplary cervical plate system (100) illustrating the components of the screw assembly (120). As shown in FIG. 2, the screw assembly (120) includes, but is in no way limited to, a lock pin (200), an expandable ring (210), and a bone screw (220). The various portions of the screw assembly (120) are selectively inserted into the thru bore(s) (230) formed in the exemplary bone plate (110). As mentioned, when fully engaged, the exemplary cervical plate system (100) is able to maintain a relatively low profile while providing structural support and preventing screw back out. A detailed description of each of the components of the exemplary cervical plate system (100) is provided below, followed by a description of their interaction during assembly.

[0022] FIGS. 3A, 3B, and 3C illustrate various views of the bone plate (110), according to one exemplary embodiment. As shown, the bone plate generally includes a main plate body (300) having a number of material cut-out(s) (310) and thru-bore(s) (230) formed therein. As illustrated, the plate body (300) of the bone plate (110) is slightly curved to follow the shape of a spinal column and may be formed out of any number of biocompatible metals including, but in no way limited to, stainless steel, titanium, or a titanium alloy. Moreover, the construction of the plate body (300) may be made of non-metal materials including, but in no way limited to, carbon reinforced Polyetheretherketone (PEEK), and the like. Additionally, as illustrated in FIGS. 3A and 3B, the plate body (300) has a beveled rounded periphery to eliminate any sharp or abrupt edges that could potentially be damaging to surrounding tissue.

[0023] The material cut-out(s) (310) formed in the plate body (300) may serve a number of purposes. According to one exemplary embodiment, the material cut-out(s) (310) may be designed to eliminate superfluous material, thereby reducing the overall weight of the bone plate (110), while maintaining the desired structural integrity. Additionally, the various material cut-out(s) (310) may be configured to facilitate handling of the bone plate (110) during installation or removal with a tool such as, but in no way limited to, forceps. Further, the material cut-out(s) (310) may also provide functional access to tissue and/or bone located behind an installed bone plate (110) without necessitating removal of the plate.

[0024] FIG. 3C is a cross-sectional view detailing an exemplary varying profile of the thru-bore (230), according to one exemplary embodiment. As shown, a plurality of thru-bores (230) are formed in the plate body (300), six in the exemplary embodiment illustrated in FIG. 3A. A pair of thru-bores (230) are formed at each of the extreme ends and the center of the plate body (300), according to the exemplary embodiment illustrated in FIG. 3A. However, any number of thru-bore configurations may be employed in the plate body (300) to accomplish varying desired coupling points.

[0025] As illustrated in the cross-sectional view of FIG. 3C, each of the exemplary thru-bore(s) (230) include a reception chamfer (320) formed at the interface with the top surface of the plate body (300). The reception chamfer (320) of the exemplary thru bore(s) (230) facilitates reception of a screw assembly (120; FIG. 2) while eliminating the formation of a sharp or potentially damaging edge at the surface of the plate body (300).

[0026] Further, as shown, the thru-bore (230) includes a varying bore profile including a top reception diameter (330), a center cavity diameter (350), and an exit diameter (340) defined by a bore stop (360). According to one exemplary embodiment, described in further detail below, both the top reception diameter (330) and the exit diameter (340) of the exemplary thru-bore(s) (230) are smaller than the central cavity diameter (350). Due to the varying bore profile, a screw assembly (120; FIG. 2) having a selectively actuated expansion member may be inserted into the thru-bore(s) (230) and the expansion member actuated to approximately the diameter of the central cavity diameter (350). According to the present exemplary embodiment, expanding the expansion member to approximately the diameter of the central cavity diameter (350) will create an interference fit between the plate body (300) and the expansion member in all directions, thereby eliminating any degrees of freedom the screw assembly (120; FIG. 2) may have relative to the plate body (300). According to another exemplary embodiment, the expansion member may be actuated to a size slightly greater than that of the reception diameter (330) yet less than the central cavity diameter (350). According to this exemplary embodiment, the size of the expansion member will prevent exit of the screw assembly (120; FIG. 1) from the thru-bore (320) while allowing for movement of the screw head within the thru-bore. This movement may be beneficial as an intermediate step when a surgeon is initially placing the bone plate.

[0027] Further, according to one exemplary embodiment, the bore stop protrusion (360) that defines the exit diameter (340) of the thru-bore (230) may cause the exit diameter to be smaller than the diameter of the head base (415; FIG. 4) of the screw assembly (120). Consequently, the screw assembly (120) may be inserted into a bone via the bone plate (110) until the head base (415; FIG. 4) is seated upon the bore stop (360). The incorporation of the bore stop provides for consistent insertion of the screw assembly (120) relative to the top surface of the bone plate (110). While the bore profile of the present exemplary thru-bore (230) is illustrated as having gradual changes in the internal diameter, abrupt or dramatic variations in profile of the thru-bore (230) may also define the thru-bore, according to one exemplary embodiment.

[0028] FIGS. 4A through 4D detail a number of elements of a bone screw (220), according to one exemplary embodiment. As illustrated, the bone screw (220) includes features generally classified as a thread portion (400) and a head portion (410). According to one exemplary embodiment, the thread portion (400) of the bone screw (220) is configured to be affixed to the bone of a patient during spine surgery. Particularly, as shown, the thread portion (400) of the exemplary bone screw (220) may include a self-tapping leading edge (450), as is best shown in FIG. 4B. According to this exemplary embodiment, the incorporation of a self-tapping leading edge in the thread portion (400) of the bone screw (220) provides the bone screw with the ability to remove bone material as it is being inserted, eliminating a step of a surgeon drilling a pilot hole prior to insertion of the bone screw.

[0029] The head portion (410) of the bone screw (220) includes a number of functional features including, but in no way limited to, a plurality of driving features (420) formed on a head base (415), a ring channel (430) formed in a side of the driving features, and a pin bore (440) extending from the center of the head portion into the center of the thread portion (400). According to the present exemplary embodiment, the head portion (410) of the bone screw (410) transitions from the thread portion (400) with the head base (415). According to one exemplary embodiment, the outer diameter of the head base (415) is larger than the outer diameter of any section of the thread portion (400). By forming the head base (415) larger than the thread portion (400) of the bone screw (220), the thread portion of the bone screw may pass through an appropriately sized thru-bore (230; FIG. 2) substantially corresponding in size with the thread portion while preventing the head base from passing there through. This configuration allows for consistent insertion depth of the bone screw (220) into a desired thru-bore (230; FIG. 2).

[0030] A number of protrusions in the form of driving features (420) are formed extending upwardly from the head base (415), according to one exemplary embodiment. As illustrated in FIGS. 4A and 4C, the shown embodiment includes three protrusions acting as driving features (420). However, any number of driving features (420) may be formed on the head base (415), according to the teachings of the present exemplary system and method. According to one exemplary embodiment, at least the upper portion of the driving features may be engaged by a corresponding driving feature during installation. According to this exemplary embodiment, the corresponding driving feature (not shown) may engage the driving features (420) and impart a rotational force thereon, driving the thread portion (400) of the bone screw (220) into a desired bone.

[0031] As illustrated in FIGS. 4A and 4D, an annular groove is formed in the driving features (420) to form a ring channel (430) around the head portion (410) just above the head base (415). According to one exemplary embodiment, the ring channel (430) formed in the driving features (420) of the present exemplary bone screw (220) is sufficiently deep to receive and house an expandable ring (210; FIG. 2) in a relaxed state and retain the expandable ring when driven open to retain the screw assembly (120; FIG. 1) in a thru-bore (230; FIG. 2).

[0032] A pin bore (440) is also formed in the exemplary bone screw (220), as is best illustrated in FIG. 4D. According to one exemplary embodiment, the pin bore (440) is formed concentric with the axis of the bone screw (220) and has a diameter substantially similar to the diameter of the lock pin (200; FIG. 2). As shown in FIG. 4D, the pin bore (440) may also correspond in height with the height of a lock pin (200; FIG. 2) to assure the lock pin may be fully inserted into the pin bore (440) during operation.

[0033] Alternatively, the pin bore (440) formed in the exemplary bone screw (220) may be formed with a height that well exceeds the height of a lock pin (200). According to this alternative embodiment, the bone screw (220) may have a pin bore (440) that extends through the entire screw height. According to this exemplary embodiment, the extended pin bore (440) not only allows for a lock pin (200) to be fully engaged to selectively expand an expandable ring (210), but also allows for a lock pin to be extended beyond the expandable ring into the pin bore (440), thereby facilitating a release of the expandable ring.

[0034] FIGS. 5A and 5B illustrate the expandable ring (210) of the screw assembly (210; FIG. 2), according to one exemplary embodiment. As shown in FIGS. 5A and 5B, the exemplary expandable ring is configured to mate with and be selectively expanded in the ring channel (430; FIG. 4A) of the bone screw (220). Specifically, the expandable ring (210) includes a substantially circular outer rib (500) having an expansion gap (505) formed therein. According to one exemplary embodiment, the expansion gap (505) is configured to facilitate the expansion and contraction of the expandable ring (210) without causing undue stresses on the member material. The width of the outer rib (500) is defined by the difference between the inner diameter (530) of the outer rib and the outer diameter (540) of the outer rib. According to one exemplary embodiment described in further detail below, the difference between the inner diameter (530) and the outer diameter (540) is such that the expandable ring (210) may be retained in the ring channel (430; FIG. 4A) of the bone screw (220; FIG. 2) in both an un-expanded state and an expanded state within a thru-bore (230; FIG. 2).

[0035] In addition to the expansion gap (505), the expandable ring (210) includes a number of expansion ribs (510) protruding from the outer rib (500) toward the center of the expandable ring. As shown, the expansion ribs (510) terminate in a lock pin engagement surface (515) and define a driving feature orifice (520) between each pair of adjacent expansion ribs and a pin orifice (530) between the lock pin engagement surfaces. According to one exemplary embodiment, the driving feature orifices (520) are configured to receive the driving features (420; FIG. 4C) formed on the head portion (410; FIG. 4A) of the bone screw (220; FIG. 2), during assembly. Additionally, the lock pin engagement surfaces (515) cause the pin orifice (530) to be concentrically aligned with the pin bore (440; FIG. 4D) when assembled. Consequently, the engagement surfaces are configured to receive a lock pin (200; FIG. 2) and translate any variations in the surface profile of the lock pin to the outer rib (500) as the lock pin is passed into the pin bore (440; FIG. 4D), thereby controlling the expansion and/or contraction of the outer rib (500).

[0036] FIGS. 6A and 6B illustrate an exemplary lock pin (200) according to one exemplary embodiment. As shown, the exemplary lock pin (200) is a substantially cylindrical member having a proximal (670) and a distal end (675). Additionally, a number of cut outs and/or tapers are formed in the lock pin (200) to create a varying outer pin diameter (680). According to the exemplary embodiment illustrated in FIGS. 6A and 6B, the lock pin (200) includes an entry taper (650) formed on the distal end (675) thereof. The entry taper (650) is a graduated surface configured to facilitate initial alignment and engagement of the lock pin (200) with both the pin orifice (530; FIG. 5A) of the expandable ring (210; FIG. 5A) and the pin bore (440; FIG. 4D) of the bone screw (220; FIG. 4D).

[0037] Moving towards the proximal end (670) of the lock pin (200), the entry taper (650) leads to an entry body (640) having a substantially consistent outer pin diameter (680) configured to at least slightly expand the expandable ring (210) during assembly. The entry body (640) leads to a retention cut-out portion (630) that defines a small diameter surface (620) of the lock pin (200). According to one exemplary embodiment, the small diameter surface (620) has a relaxed diameter (625) substantially corresponding to the pin orifice (530; FIG. 5A) in a relaxed or near relaxed expandable ring state. According to one exemplary embodiment, when the screw assembly (120; FIG. 2) is assembled, the expandable ring (210) engages the small diameter surface (620), allowing the expandable ring to remain in a relaxed state until fully engaged.

[0038] Continuing towards the proximal end (670) of the lock pin (200), a graduated expansion surface (610) extends from the small diameter surface (620), terminating in the lock surface (600) portion of the lock pin (200). During a locking step of the present exemplary system, the lock pin (200) is advanced in the pin bore (440; FIG. 4D) such that the lock pin engagement surfaces (515; FIG. 5A) of the expandable ring (210) engage the graduated expansion surface (610) and the lock surface (600) to expand the expandable ring to an appropriate diameter within the thru-bore (230; FIG. 2). According to one exemplary embodiment, the outer pin diameter (680) of the lock surface (600) is sufficient to expand the expandable ring (210; FIG. 2) to a desired friction inducing state, while still constraining the expandable ring in the ring channel (430; FIG. 4A) and without permanently deforming the expansion ring. Further detail of the function and operation of the exemplary cervical plate system (100) will be described below with reference to FIGS. 7-11.

Exemplary Method (not forming part of the present invention)

[0039] FIG. 7 illustrates a method for installing the exemplary cervical plate system (100; FIG. 1), according to one exemplary embodiment. As illustrated in FIG. 7, the present exemplary method for installing the cervical plate system (100; FIG. 1) includes placing the bone plate adjacent to one or more desired vertebral bones (step 700). Once the bone plate is appropriately positioned, the screw assembly may then be presented to a thru-bore of the bone plate with the expandable ring in a relaxed state at a small diameter (step 710). The screw assembly is then driven through the thru-bore in the bone plate into the desired vertebral bone (step 720) until the enlarged head of the screw assembly is within the central cavity of the thru-bore, seated on the bore stop (step 730). Once the screw assembly is correctly positioned, the lock pin may be translated to enlarge the diameter of the expandable ring, thereby capturing the screw assembly within the thru-bore (step 740). Further details of each step of the present exemplary method will be provided below with reference to FIGS. 8 through 11.

[0040] As illustrated in FIG. 7, the first step of the exemplary method is to place the plate adjacent to a desired vertebral bone (step 700). The placement of the bone plate (110; FIG. 1) relative to a vertebral bone in a patient may be pre-operatively determined based on a pre-operative examination of the patient's spinal system using non-invasive imaging techniques known in the art, such as x-ray imaging, magnetic resonance imaging (MRI), and/or fluoroscopy imaging, for example. Any additional preparation or work may be done on and around the desired vertebral bone prior to positionally orienting the bone plate. As illustrated in FIG. 8, the bone plate (110) is oriented such that the reception chamfer (320) is facing away from the desired bone, facilitating insertion of the present screw assembly.

[0041] With the bone plate appropriately positioned relative to a desired vertebral bone (step 700), the screw assembly may be presented to a thru-bore of the bone plate with the expandable ring in a relaxed state (step 710). As shown in FIG. 9, the screw assembly (120) may be delivered to the surgeon as a three piece assembly including the bone screw (220), the expandable ring (210), and the lock pin (200). According to the illustrated exemplary embodiment, when delivered to the surgeon, the lock pin (200) is undeployed and the expandable ring (210) is in a relaxed state. More specifically, according to one exemplary embodiment, the small diameter surface (620; FIG. 6A) of the lock pin (200) is engaged with the lock pin engagement surfaces (515; FIG. 5A) of the expandable ring (210). Maintaining the screw assembly (120) in this configuration during delivery and storage prevents any permanent deformation of the expandable ring (210) due to creep and other material phenomena.

[0042] When presented, the screw assembly (120) may then be driven through the thru-bore (230) in the bone plate (110) into a desired vertebral bone (step 720). As mentioned, the screw assembly may be driven into the desired vertebral bone by coupling a driving tool to the driving features (420) of the bone screw (220). Once mating, the driving tool may impart a rotational force on the head portion (410) of the bone screw (220). Consequently, the self-tapping thread portion (400; FIG. 4A) of the bone screw (220) will remove bone material as it advances into the desired bone. The screw assembly (120) may be partially driven initially if multiple screw assemblies (120) are to be inserted in a single bone plate (110) or if further work is to be done by a surgeon prior to final assembly.

[0043] The screw assembly (120) may be driven through the thru-bore (230) until the head portion (410) of the bone screw (220) is within the central cavity of the thru-bore (step 730). As mentioned previously, consistent seating of the screw assembly (120) in the thru-bore (230) may be accomplished by driving the bone screw (220) into the thru-bore (230) until the head base (415; FIG. 4A) of the bone screw seats upon the bore stop (360; FIG. 3C) within the thru-bore. FIG. 10 illustrates a screw assembly (120) seated in the thru-bore (230) as described above. As shown, by driving the bone screw (220) into the thru-bore (230) until the head base (415; FIG. 4A) of the bone screw seats upon the bore stop (360; FIG. 3C), the top surface of the head portion (410; FIG. 4A) is driven to or below the top surface of the bone plate (110).

[0044] Once the screw assembly is correctly positioned in the thru-bore (230), the lock pin (200) may be engaged to enlarge the diameter of the expandable ring (210), capturing the screw within the thru-bore (step 740), as illustrated in FIG. 11. As mentioned previously, the lock pin (200) is engaged by applying a downward force (F1) to the lock pin (200). As the lock pin (200) is translated into the pin bore (440), the expansion ring (210) is acted upon by the varying profile of the lock pin. Specifically, the graduated expansion surface (610; FIG. 6A) of the lock pin (200) will impart an increasing force on the expansion ring (210) until the lock pin is fully engaged and the lock surface (600) is imparting a desired outward force upon the expansion ring. While an axial translation of the lock pin imparts a radial force on the expansion ring of the exemplary embodiment detailed herein, movement of the lock pin is in no way limited to an axial translation. Rather, by way of example, a lock pin having a non-circular cross-sectional profile, such as a triangle or other lobed profile, may be rotated within the pin bore (440) to impart a changing radial force on the expansion ring. In response to the increased outward force exerted by the lock surface (600) of the lock pin (200) upon the expansion ribs (540; FIG. 5A) of the expansion ring (210), the diameter of the expansion ring is enlarged about the head portion (410; FIG. 4A) of the bone screw assembly (120). The enlarging of the expansion ring (210) about the head portion (410; FIG. 4A) of the bone screw assembly (120) imparts an outward force (F2) from the expansion ring to the inner surface of the thru-bore (230). According to one exemplary embodiment, the outward force (F2) exerted by the expansion ring (210) to the thru-bore (230) creates a frictional fit that captures the bone screw (220) within the thru-bore of the bone plate. Further, as mentioned above, the outer diameter of the expansion ring (210) in its expanded state is larger than both the reception diameter (330; FIG. 3C) and the exit diameter (340; FIG. 3C) of the exemplary thru-bore (230). Consequently, the bone screw assembly (120) is prevented from backing out from, or further advancing in the thru-bore (230).

[0045] While the present exemplary orthopedic plate system (100; FIG. 1) has been described, for ease of explanation only, in the context of a cervical plate system, the present exemplary systems and methods may be applied to any number of orthopedic fixtures. Specifically, the present bone screw assembly (120) may be used to couple any number of orthopedic apparatuses to a desired bone, for any number of purposes, as long as the connecting orthopedic apparatus includes a thru-bore substantially conforming with the configurations described herein.

[0046] In conclusion, the present exemplary systems and methods provide for coupling an orthopedic plate to one or more bones while preventing back-out of the fastener. Particularly, the present exemplary system is configured to leverage the varying bore diameter of a thru-bore formed in the bone plate to prevent the screw system from backing out while utilizing a minimal engagement surface on the bone plate. Consequently, the profile size of the bone plate, when compared to traditional orthopedic plate systems, is reduced and the dangers associated with screw back-out are reduced. This reduction in profile size adds comfort to the patient by reducing the likelihood that difficulty in swallowing will develop due to the presence of the orthopedic plate system.

[0047] The preceding description has been presented only to illustrate and describe the present system. It is not intended to be exhaustive or to limit the present system to any precise form disclosed.

[0048] The foregoing embodiments were chosen and described in order to illustrate principles of the system as well as some practical applications. The preceding description enables others skilled in the art to utilize the system in various embodiments and with various modifications as are suited to the particular use contemplated. It is intended that the scope of the present exemplary system be defined by the following claims.

Claims

1. A bone fixation system (100) comprising:

a bone plate (110) including a thru-bore (230) having an entry diameter (330), an intermediate diameter (350), and an exit diameter (340), wherein said intermediate diameter (350) is larger than said entry diameter (330) and said exit diameter (340); and

a bone screw assembly (120) configured to be coupled to said thru-bore (230);

wherein said screw assembly (120) comprises:

a bone screw (220) having a head section (410), a thread section (400), and a central bore (440);

an expandable ring (210) coupled to said head section (410); and

a pin (200) arranged to be at least partially disposed in said central bore (440);

wherein said pin (200) includes a varying outer profile (680) that engages said expandable ring (210) to vary an outer diameter (540) of said expandable ring (210) to couple said screw assembly (120) in said thru-bore (230);

and the head section (410) further comprising a ring channel (430) configured to retain said expandable ring (210) in both a relaxed position and an expanded position and wherein said pin (200) comprises:

a generally cylindrical body having a proximal end (670) and a distal end (675);

a graduated entry taper (650) formed on said distal end (675);

a first engagement diameter (625) disposed along said body, wherein said first engagement diameter (625) corresponds to a relaxed diameter (625) of said expandable ring (210); and

a second engagement diameter (680) disposed along said body between said first engagement diameter (625) and said proximal end (670) of said pin (210), wherein said second engagement diameter (680) corresponds to an expanded diameter of said expandable ring (210).

2. The bone fixation system (100) of claim 1, wherein said bone plate (110) includes a plurality of said thru-bores (230).

3. The bone fixation system of claim 1, further comprising a plurality of driving protrusions (420) extending from said head section (410), having overhang members defining the ring channel (430).

4. The bone fixation system (100) of claim 1, wherein said central bore (440) extends along an entire axial length of said bone screw (220).

5. The bone fixation system (100) of claim 1, wherein said expandable ring (210) comprises an outer member including an expansion relief (505).

6. The bone fixation system (100) of claim 5, wherein said expandable ring (210) further comprises a plurality of protrusions extending inwardly from said outer member (500);
wherein said plurality of protrusions (510) contact an outer surface (680) of said pin (200) and transfer variations in said outer surface (680) to said outer member (500).

7. The orthopedic bone fixation system (100) of claim 1, wherein said thru-bore (230) further comprises an annular bore stop protrusion (360) defining said exit diameter (340).

8. The bone fixation system (100) of claim 1, wherein said bone plate (110) comprises:

a curved body;

a plurality of said thru-bores (230) defined by said body; and

a plurality of cut-out orifices (310) defined by said body.

9. The bone fixation system (100) of claim 1, further comprising a graduated transition surface (610) disposed between said first engagement diameter (625) and said second engagement diameter (680).

Ansprüche

1. Knochenfixationssystem (100), das Folgendes umfasst:

eine Knochenplatte (110) mit einer Durchgangsbohrung (230) mit einem Eintrittsdurchmesser (330), einem Zwischendurchmesser (350) und einem Austrittsdurchmesser (340), wobei der genannte Zwischendurchmesser (350) größer ist als der genannte Eintrittsdurchmesser (330) und der genannte Austrittsdurchmesser (340); und

eine Knochenschraubenbaugruppe (120), die zum Koppeln mit der genannten Durchgangsbohrung (230) konfiguriert ist;

wobei die genannte Schraubenbaugruppe (120) Folgendes umfasst:

eine Knochenschraube (220) mit einem Kopfabschnitt (410), einem Gewindeabschnitt (400) und einer zentralen Bohrung (440);

einen expandierbaren Ring (210), der mit dem genannten Kopfabschnitt (410) gekoppelt ist; und

einen Stift (200), der so ausgelegt ist, dass er wenigstens teilweise in der genannten zentralen Bohrung (440) aufgenommen wird;

wobei der genannte Stift (200) ein variierendes Außenprofil (680) hat, das in den genannten expandierbaren Ring (210) eingreift, um einen Außendurchmesser (540) des genannten expandierbaren Rings (210) zu variieren, um die genannte Schraubenbaugruppe (120) in der genannten Durchgangsbohrung (230) zu koppeln;

wobei der Kopfabschnitt (410) ferner einen Ringkanal (430) umfasst, der so konfiguriert ist, dass er den expandierbaren Ring (210) sowohl in einer entspannten Position als auch in einer expandierten Position hält, und wobei der genannte Stift (200) Folgendes umfasst:

einen allgemein zylindrischen Körper mit einem proximalen Ende (670) und einem distalen Ende (675);

einen abgestuften Eintrittskegel (650), der an dem genannten distalen Ende (675) ausgebildet ist;

einen ersten Eingriffsdurchmesser (625), der entlang dem genannten Körper angeordnet ist, wobei der genannte erste Eingriffsdurchmesser (625) einem entspannten Durchmesser (625) des genannten expandierbaren Rings (210) entspricht; und

einen zweiten Eingriffsdurchmesser (680), der entlang dem genannten Körper zwischen dem genannten ersten Eingriffsdurchmesser (625) und dem genannten proximalen Ende (670) des genannten Stifts (210) angeordnet ist, wobei der genannte zweite Eingriffsdurchmesser (680) einem expandierten Durchmesser des genannten expandierbaren Rings (210) entspricht.

2. Knochenfixationssystem (100) nach Anspruch 1, wobei die genannte Knochenplatte (110) mehrere genannte Durchgangsbohrungen (230) aufweist.

3. Knochenfixationssystem nach Anspruch 1, das ferner mehrere Treibvorsprünge (420) aufweist, die sich von dem genannten Kopfabschnitt (410) erstrecken und Überhangelemente aufweisen, die den Ringkanal (430) definieren.

4. Knochenfixationssystem (100) nach Anspruch 1, wobei die genannte zentrale Bohrung (440) über eine gesamte axiale Länge der genannten Knochenschraube (220) verläuft.

5. Knochenfixationssystem (100) nach Anspruch 1, wobei der genannte expandierbare Ring (210) ein Außenelement mit einer Expansionsaussparung (505) umfasst.

6. Knochenfixationssystem (100) nach Anspruch 5, wobei der genannte expandierbare Ring (210) ferner mehrere Vorsprünge umfasst, die von dem genannten Außenelement (500) nach innen verlaufen;
wobei die genannten mehreren Vorsprünge (510) eine Außenfläche (680) des genannten Stifts (200) kontaktieren und Variationen in der genannten Außenfläche (680) auf das genannte Außenelement (500) übertragen.

7. Orthopädisches Knochenfixationssystem (100) nach Anspruch 1, wobei die genannte Durchgangsbohrung (230) ferner einen ringförmigen Bohrungsanschlagvorsprung (360) umfasst, der den genannten Ausgangsdurchmesser (340) definiert.

8. Knochenfixationssystem (100) nach Anspruch 1, wobei die genannte Knochenplatte (110) Folgendes umfasst:

einen gekrümmten Körper;

mehrere genannte Durchgangsbohrungen (230), die von dem genannten Körper definiert werden; und

mehrere Ausschnittsöffnungen (310), die von dem genannten Körper definiert werden.

9. Knochenfixationssystem (100) nach Anspruch 1, das ferner eine abgestufte Übergangsfläche (610) aufweist, die zwischen dem genannten ersten Eingriffsdurchmesser (625) und dem genannten zweiten Eingriffsdurchmesser (680) angeordnet ist.

Revendications

1. Système de fixation osseuse (100), comprenant
une plaque osseuse (110) comprenant un trou traversant (230) doté d'un diamètre d'entrée (330), un diamètre intermédiaire (350) et un diamètre de sortie (340), où ledit diamètre intermédiaire (350) est supérieur audit diamètre d'entrée (330) et audit diamètre de sortie (340) ; et
un ensemble vis à os (120) configuré pour être couplé audit trou traversant (230) ;
où ledit ensemble vis (120) comprend :

une vis à os (220) dotée d'une section de tête (410), une section filetée (400) et

un trou central (440) ;

un anneau expansible (210) couplé à ladite section de tête (410) ; et

un goujon (200) prévu pour être au moins partiellement disposé dans ledit trou central (440) ;

où ledit goujon (200) comprend un profil extérieur variable (680) qui engage ledit anneau expansible (210) pour faire varier un diamètre extérieur (540) dudit anneau expansible (210) afin de coupler ledit ensemble vis (120) dans

ledit trou traversant (230) ;

et où la section de tête (410) comprend de plus un canal annulaire (430) configuré pour retenir ledit anneau expansible (210) dans une position détendue ainsi qu'une position expansée et où ledit goujon (200) comprend :

un corps généralement cylindrique doté d'une extrémité proximale (670) et

une extrémité distale (675) ;

un cône d'entrée graduelle (650) formé sur ladite extrémité distale (675) ;

un premier diamètre d'engagement (625) disposé le long dudit corps, où ledit premier diamètre d'engagement (625) correspond à un diamètre détendu (625) dudit anneau expansible (210) ; et

un deuxième diamètre d'engagement (680) disposé le long dudit corps entre ledit premier diamètre d'engagement (625) et ladite extrémité proximale (670) dudit goujon (210), où ledit deuxième diamètre d'engagement (680) correspond à un diamètre expansé dudit anneau expansible (210).

2. Système de fixation osseuse (100) selon la revendication 1, où ladite plaque osseuse (110) comprend une pluralité desdits trous traversants (230).

3. Système de fixation osseuse selon la revendication 1, comprenant de plus une pluralité de protubérances d'entraînement (420) s'étendant depuis ladite section de tête (410), dotées d'éléments en surplomb définissant le canal annulaire (430).

4. Système de fixation osseuse (100) selon la revendication 1, où ledit trou central (440) s'étend le long de la totalité d'une longueur axiale de ladite vis à os (220).

5. Système de fixation osseuse (100) selon la revendication 1, où ledit anneau expansible (210) comprend un élément extérieur comprenant une libération d'expansion (505).

6. Système de fixation osseuse (100) selon la revendication 5, où ledit anneau expansible (210) comprend de plus une pluralité de protubérances s'étendant vers l'intérieur depuis ledit élément extérieur (500) ;
où ladite pluralité de protubérances (510) contactent une surface extérieure (680) dudit goujon (200) et transfèrent les variations de ladite surface extérieure (680) audit élément extérieur (500).

7. Système de fixation osseuse orthopédique (100) selon la revendication 1, où ledit trou traversant (230) comprend de plus une protubérance d'arrêt de trou annulaire (360) définissant ledit diamètre de sortie (340).

8. Système de fixation osseuse (100) selon la revendication 1, où ladite plaque osseuse (110) comprend :

un corps courbe ;

une pluralité desdits trous traversants (230) définis par ledit corps ; et

une pluralité d'orifices découpés (310) définis par ledit corps.

9. Système de fixation osseuse (100) selon la revendication 1, comprenant de plus une surface de transition graduelle (610) disposée entre ledit premier diamètre d'engagement (625) et ledit deuxième diamètre d'engagement (680).

Drawing